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Volumn 52, Issue 2, 2000, Pages 707-717

Novel synthesis of 1-fluoro-1-silyloxiranes using bromo(tert- butyldimethylsilyl)fluoromethyllithium and carbonyl compounds

Author keywords

[No Author keywords available]

Indexed keywords

BROMO(TERT BUTYLDIMETHYLSILY)FLUOROMETHYLLITHIUM; CARBONYL DERIVATIVE; ETHYLENE OXIDE; LITHIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0034143370     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-99-S74     Document Type: Article
Times cited : (9)

References (41)
  • 13
    • 0001329712 scopus 로고
    • ed. by S. Patai and Z. Rappoport, John Wiley & Sons, Inc., New York
    • a) A. R. Bassindale and P. G. Taylor, 'The Chemistry of Organic Silicon Compounds,' Vol. 2, ed. by S. Patai and Z. Rappoport, John Wiley & Sons, Inc., New York, 1989, pp. 893-963;
    • (1989) The Chemistry of Organic Silicon Compounds , vol.2 , pp. 893-963
    • Bassindale, A.R.1    Taylor, P.G.2
  • 14
    • 0001172865 scopus 로고
    • ed. by B. M. Trost and I. Fleming, Pergamon Press, London
    • b) J. S. Panek, 'Comprehensive Organic Synthesis,' Vol. 1, ed. by B. M. Trost and I. Fleming, Pergamon Press, London, 1991, pp. 579-627.
    • (1991) Comprehensive Organic Synthesis , vol.1 , pp. 579-627
    • Panek, J.S.1
  • 29
    • 0030580396 scopus 로고    scopus 로고
    • 3)Li which could be prepared at -78 °C and was alkylated with alkyl iodides in good yields
    • 3)Li which could be prepared at -78 °C and was alkylated with alkyl iodides in good yields.
    • (1996) Tetrahedron , vol.52 , pp. 14533
    • Shinokubo, H.1    Oshima, K.2    Utimoto, K.3
  • 35
    • 0342829956 scopus 로고
    • Although 1,2-difluoro-1-silyloxiranes and 1,2,2-trifluoro-1-silyloxirane were reportedly prepared by epoxidation of the corresponding fluorosilylethenes (vide infra), the synthesis of 1-fluoro-1-silyloxiranes (5) has never been reported, to the best of our knowledge, a) T. Dubuffet, R. Sauvetre, and J.-F. Normant, J. Organomet. Chem., 1988, 354, 1;
    • (1988) J. Organomet. Chem. , vol.354 , pp. 1
    • Dubuffet, T.1    Sauvetre, R.2    Normant, J.-F.3
  • 37
    • 0343322220 scopus 로고    scopus 로고
    • note
    • No product resulting from the Peterson elimination or the Brook rearrangement of 8 was observed.
  • 39
    • 0001391988 scopus 로고
    • ed. by D. Barton and W. D. Ollis, Pergamon Press, Oxford
    • a) I. Fleming, 'Comprehensive Organic Chemistry,' Vol. 3, ed. by D. Barton and W. D. Ollis, Pergamon Press, Oxford, 1979, pp. 541-686;
    • (1979) Comprehensive Organic Chemistry , vol.3 , pp. 541-686
    • Fleming, I.1
  • 40
    • 0343758214 scopus 로고    scopus 로고
    • Ref. 5a; pp. 951-955
    • b) Ref. 5a; pp. 951-955.
  • 41
    • 0343322219 scopus 로고    scopus 로고
    • note
    • When i-propyl iodide or i-butyl iodide was used, protonated product (6) (R″ = H) formed which might have resulted from a proton abstraction from the iodide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.